medical Class III Updated 2019-04-24

Aniara Diagnostica LLC recalls BIOPHEN UFH Control C2, REF 223901

Recalled Product

BIOPHEN UFH Control C2, REF 223901

Hazard / Issue

The manufacturer packaged incorrect versions of the Instructions for Use into specific lots for three device product codes.

Issued by

FDA

Affected States: MI, PA
Lot/Code Info: Lot F1700315P7
View official government recall

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